Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762265Generated: October 30, 2026

5-Chloro-2-fluoro-3-nitropyridine → 5-Chloro-2-fluoropyridin-3-amine

https://huagongshe.com/reaction/1762265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-fluoro-3-nitropyridineHCID 12275768—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-Chloro-2-fluoropyridin-3-amineHCID 2004288876.4%

Reaction Steps

7.5 g (0.042 mol) of 5-chloro-2-fluoro-3-nitropyridine are dissolved in 80 ml of ethanol. This solution is hydrogenated with hydrogen, in the presence of 1 g of Raney nickel catalyst, under normal pressure and at a temperature in the range from 20° to 25° C. After a hydrogenation period of 20 hours, the catalyst is removed and the solvent is evaporated off. The residue is taken up in ethyl acetate and the resultant solution is filtered through a layer of silica gel. The solvent is evaporated off and the residue is triturated in hexane. The precipitate is subsequently filtered and dried, affording 4.7 g (76%) of 3-amino-5-chloro-2-fluoropyridine, m.p. 74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831148
Source datasetuspto-grants-1989_05
ORD IDord-2e2791366d20469bbd666d7609e23186
Source noteuspto-grants-1989_05